Canonical Allele Identifier: CA366468001

Gene: WDR27

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169659092G>C , CM000668.2:g.169659092G>C	GRCh38
NC_000006.11:g.170059188G>C , CM000668.1:g.170059188G>C	GRCh37
NC_000006.10:g.169801113G>C	NCBI36
NG_046155.1:g.47972C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448612.6:c.1313C>G MANE Select	ENSP00000416289.1:p.Pro438Arg
ENST00000647790.1:c.*2096C>G	ENSP00000498206.1:n.*2096C>G
ENST00000647873.1:c.1109C>G	ENSP00000497692.1:p.Pro370Arg
ENST00000647889.1:c.*3242C>G	ENSP00000497364.1:n.*3242C>G
ENST00000648086.1:c.331+13163C>G	ENSP00000497979.1:n.331+13163C>G
ENST00000648472.1:c.*358+359C>G	ENSP00000496961.1:n.*358+359C>G
ENST00000649303.1:c.*612C>G	ENSP00000497180.1:n.*612C>G
ENST00000649579.1:c.210C>G	ENSP00000497123.1:p.Ala70=
ENST00000650382.1:n.109-24567C>G
ENST00000423258.5:c.932C>G	ENSP00000397869.1:p.Pro311Arg
ENST00000441385.2:c.214C>G
ENST00000448612.5:c.1313C>G	ENSP00000416289.1:p.Pro438Arg
ENST00000467418.1:n.570C>G
ENST00000546525.5:n.828C>G
NM_001202550.1:c.932C>G	NP_001189479.1:p.Pro311Arg
NM_182552.4:c.1313C>G	NP_872358.4:p.Pro438Arg
XM_011535682.1:c.1313C>G	XP_011533984.1:p.Pro438Arg
XM_011535683.1:c.1313C>G	XP_011533985.1:p.Pro438Arg
XM_011535684.1:c.1313C>G	XP_011533986.1:p.Pro438Arg
XM_011535685.1:c.1313C>G	XP_011533987.1:p.Pro438Arg
XM_011535686.1:c.1313C>G	XP_011533988.1:p.Pro438Arg
XM_011535687.1:c.1313C>G	XP_011533989.1:p.Pro438Arg
XM_011535688.1:c.1313C>G	XP_011533990.1:p.Pro438Arg
XM_011535689.1:c.1313C>G	XP_011533991.1:p.Pro438Arg
XM_011535690.1:c.1313C>G	XP_011533992.1:p.Pro438Arg
XM_011535691.1:c.1313C>G	XP_011533993.1:p.Pro438Arg
XM_011535692.1:c.1313C>G	XP_011533994.1:p.Pro438Arg
XM_011535693.1:c.1313C>G	XP_011533995.1:p.Pro438Arg
XM_011535694.1:c.1313C>G	XP_011533996.1:p.Pro438Arg
XM_011535695.1:c.1313C>G	XP_011533997.1:p.Pro438Arg
XM_011535696.1:c.1313C>G	XP_011533998.1:p.Pro438Arg
XM_011535697.1:c.1313C>G	XP_011533999.1:p.Pro438Arg
XR_942377.1:n.1320C>G
XR_942378.1:n.1320C>G
XR_942379.1:n.1320C>G
XR_942380.1:n.1320C>G
XR_942381.1:n.1320C>G
XR_942382.1:n.1320C>G
XR_942383.1:n.1320C>G
NM_001350623.1:c.740C>G	NP_001337552.1:p.Pro247Arg
NM_001350624.1:c.1109C>G	NP_001337553.1:p.Pro370Arg
NM_001350625.1:c.1109C>G	NP_001337554.1:p.Pro370Arg
NR_146875.1:n.1447+359C>G
NR_146876.1:n.2331C>G
XM_011535682.3:c.1313C>G	XP_011533984.1:p.Pro438Arg
XM_011535684.3:c.1313C>G	XP_011533986.1:p.Pro438Arg
XM_011535685.3:c.1313C>G	XP_011533987.1:p.Pro438Arg
XM_011535687.3:c.1313C>G	XP_011533989.1:p.Pro438Arg
XM_011535688.3:c.1313C>G	XP_011533990.1:p.Pro438Arg
XM_011535689.3:c.1313C>G	XP_011533991.1:p.Pro438Arg
XM_011535690.3:c.1313C>G	XP_011533992.1:p.Pro438Arg
XM_011535691.3:c.1313C>G	XP_011533993.1:p.Pro438Arg
XM_011535692.3:c.1313C>G	XP_011533994.1:p.Pro438Arg
XM_011535693.3:c.1313C>G	XP_011533995.1:p.Pro438Arg
XM_011535694.3:c.1313C>G	XP_011533996.1:p.Pro438Arg
XM_011535696.3:c.1313C>G	XP_011533998.1:p.Pro438Arg
XM_011535697.3:c.1313C>G	XP_011533999.1:p.Pro438Arg
XM_017010658.2:c.1313C>G	XP_016866147.1:p.Pro438Arg
XM_017010659.2:c.1313C>G	XP_016866148.1:p.Pro438Arg
XM_017010660.2:c.1313C>G	XP_016866149.1:p.Pro438Arg
XM_017010662.2:c.1313C>G	XP_016866151.1:p.Pro438Arg
XM_017010663.2:c.1313C>G	XP_016866152.1:p.Pro438Arg
XM_017010664.2:c.1313C>G	XP_016866153.1:p.Pro438Arg
XM_017010665.2:c.1313C>G	XP_016866154.1:p.Pro438Arg
XM_017010666.2:c.1313C>G	XP_016866155.1:p.Pro438Arg
XM_017010667.2:c.1313C>G	XP_016866156.1:p.Pro438Arg
XM_017010668.2:c.1313C>G	XP_016866157.1:p.Pro438Arg
XM_017010669.2:c.740C>G	XP_016866158.1:p.Pro247Arg
XM_017010670.2:c.1313C>G	XP_016866159.1:p.Pro438Arg
XM_017010671.2:c.1313C>G	XP_016866160.1:p.Pro438Arg
XM_017010672.2:c.1313C>G	XP_016866161.1:p.Pro438Arg
XM_017010673.2:c.1313C>G	XP_016866162.1:p.Pro438Arg
NM_182552.5:c.1313C>G MANE Select	NP_872358.4:p.Pro438Arg
NM_001350623.2:c.740C>G	NP_001337552.1:p.Pro247Arg
NM_001202550.2:c.932C>G	NP_001189479.1:p.Pro311Arg
NM_001350624.2:c.1109C>G	NP_001337553.1:p.Pro370Arg
NM_001350625.2:c.1109C>G	NP_001337554.1:p.Pro370Arg
NR_146875.2:n.1413+359C>G
NR_146876.2:n.2297C>G